rs876660228

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TC)	6	BRCA2 variant considered pathogenic for breast cancer
(TC;TC)	0	common in clinvar

Make rs876660228(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32339552

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876660228
dbSNP (classic)	rs876660228
ClinGen	rs876660228
ebi	rs876660228
HLI	rs876660228
Exac	rs876660228
Gnomad	rs876660228
Varsome	rs876660228
LitVar	rs876660228
Map	rs876660228
PheGenI	rs876660228
Biobank	rs876660228
1000 genomes	rs876660228
hgdp	rs876660228
ensembl	rs876660228
geneview	rs876660228
scholar	rs876660228
google	rs876660228
pharmgkb	rs876660228
gwascentral	rs876660228
openSNP	rs876660228
23andMe	rs876660228
SNPshot	rs876660228
SNPdbe	rs876660228
MSV3d	rs876660228
GWAS Ctlg	rs876660228

Max Magnitude

6

aka c.5193_5194delTC

ClinVar
Risk	rs876660228(-;-)
Alt	rs876660228(-;-)
Reference	Rs876660228(TC;TC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32913689_32913690delTC
CLNSRC
CLNACC	RCV000218209.1,